Widespread Evolutionary Conservation of Alternatively Spliced Exons in Caenorhabditis (Irimia et al., Molecular Biology and Evolution, 2007) Note: This report shows that alternative splicing is evolutionaarily conserved in many Caenorhabditis species. Terms: cassette exons -- as an internal exon that can be either included or completely spliced out from the mRNA transcripts (i.e., not considering cases that are due to use of AS boundaries).; constitutive exons -- those exons included in all transcripts. Exons can also be divided into major forms & minor forms.
Alternative splicing in C. elegans (Alan Zahler, WormBook, 2005) Note: This reviews describes reviews that genes are alternatively spliced in tissue-specific, developmentally-regulated, and hormone-responsive manners, providing an additional mechanism for regulation of gene expression.
Large-scale RACE approach for proactive experimental definition of C. elegans ORFeome (Salehi-Ashtiani et al., Genome Research, 2009) Note: This project was initiated based on the argument that "a full third of the ORFeome remains experimentally unverified".It expermentally examined ~2,000 unverified protein-coding genes using RACE and reconstructed ORF for close to 1,000. The method RACE was chosen since "RACE (rapid amplification of cDNA ends) (Bao and Hull 1993) can proactively explore protein-coding transcript models. Large-scale RACE has been hampered by low throughput, low specificity and sensitivity, and occasionally false capture of transcript ends." This project also reported the identificaiton of SL1, SL2, & alternative trans-splicing.
C. elegans ORFeome Version 3.1: Increasing the Coverage of ORFeome Resources With Improved Gene Predictions (Lamesch et al., Genome Research, 2004) Note: This ORFeome project was based on WS100, attempting to PCR amplify ~4200 ORFs missed in earlier attempts and for which new predictions were availabe in WS100. This effort helped to increase the ORFeome size to ~12,500 ORFs (Version 3.1). The paper argues that the application of comparative genomics analysis between C. elegans & C. briggsae will help improve C. elegans gene annotation.
Massively parallel sequencing of the polyadenylated transcriptome of C. elegans (Hillier et al., Genome Research, 2009) Note: Applying Solexa sequencing method (Illumina 1G, 36-base reads), this project provided support to many splice junctions, raising the confirmed splice junctions from 70,911 to 98,000 in C. elegans. Additional, the reads suggest at least 80 putative genes not found in any predicted gene sets. Furthermore, it identifies 10,778 SL1 & 2515 SL2 signals.
Transcriptome analysis for Caenorhabditis elegans based on novel expressed sequence tags (Shin et al., Genome Biology,2008) Note: This study mapped 0.3 million 454 reads (each ~100 bp) to the C. elegans transcriptome & genome. The analysis confirmed many predicted gene, suggested the existence of novel genes and extension to existing genes, and identived L1-enriched genes. Since the library is 3'-transcript biased, there was not analysis of trans-splice sites. Before this project, WormBase contained 0.34 million ESTs obtained using the Sanger sequencing method.